Literature DB >> 11172496

Bioelectronic detection of point mutations using discrimination of the H63D polymorphism of the Hfe gene as a model.

R M Umek1, S S Lin, Y Chen Yp, B Irvine, G Paulluconi, V Chan, Y Chong, L Cheung, J Vielmetter, D H Farkas.   

Abstract

BACKGROUND: A bioelectronic detection platform has recently been developed that facilitates the detection and characterization of nucleic acids. The DNA chip platform is compatible with homogeneous assays because separate labeling and wash steps are not required. A one-step, bioelectronic detection assay was developed to genotype patient samples with respect to the H63D polymorphism of the Hfe gene, associated with hereditary hemochromatosis. METHODS AND
RESULTS: Electrode arrays were modified with DNA capture probes that were perfectly matched to the wild-type or mutant allele of H63D. Amplicons containing the polymorphic site were hybridized with the capture probes on the electrode arrays in the presence of electronically labeled reporter (signaling) probes. Voltammetric analysis of the electrode arrays was conducted first at ambient temperature and then at elevated temperature. The electronic signal was preferentially diminished at elevated temperature from electrodes that hybridized with mismatched target amplicons.
CONCLUSION: An assay for bioelectronic genotyping of the H63D polymorphism was developed and used with six patient specimens to show the feasibility of this system as a model for point mutation detection.

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Year:  2000        PMID: 11172496     DOI: 10.1007/bf03262093

Source DB:  PubMed          Journal:  Mol Diagn        ISSN: 1084-8592


  2 in total

1.  A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Authors:  J N Feder; A Gnirke; W Thomas; Z Tsuchihashi; D A Ruddy; A Basava; F Dormishian; R Domingo; M C Ellis; A Fullan; L M Hinton; N L Jones; B E Kimmel; G S Kronmal; P Lauer; V K Lee; D B Loeb; F A Mapa; E McClelland; N C Meyer; G A Mintier; N Moeller; T Moore; E Morikang; C E Prass; L Quintana; S M Starnes; R C Schatzman; K J Brunke; D T Drayna; N J Risch; B R Bacon; R K Wolff
Journal:  Nat Genet       Date:  1996-08       Impact factor: 38.330

2.  Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.

Authors:  D G Wang; J B Fan; C J Siao; A Berno; P Young; R Sapolsky; G Ghandour; N Perkins; E Winchester; J Spencer; L Kruglyak; L Stein; L Hsie; T Topaloglou; E Hubbell; E Robinson; M Mittmann; M S Morris; N Shen; D Kilburn; J Rioux; C Nusbaum; S Rozen; T J Hudson; R Lipshutz; M Chee; E S Lander
Journal:  Science       Date:  1998-05-15       Impact factor: 47.728

  2 in total
  3 in total

1.  Ultraspecific analyte detection by direct kinetic fingerprinting of single molecules.

Authors:  Tanmay Chatterjee; Zi Li; Kunal Khanna; Karen Montoya; Muneesh Tewari; Nils G Walter; Alexander Johnson-Buck
Journal:  Trends Analyt Chem       Date:  2019-12-04       Impact factor: 12.296

2.  Biosensors for Point Mutation Detection.

Authors:  Hanlin Jiang; Hui Xi; Mario Juhas; Yang Zhang
Journal:  Front Bioeng Biotechnol       Date:  2021-12-15

3.  Bioelectronic DNA detection of human papillomaviruses using eSensor: a model system for detection of multiple pathogens.

Authors:  Suzanne D Vernon; Daniel H Farkas; Elizabeth R Unger; Vivian Chan; Donna L Miller; Yin-Peng Chen; Gary F Blackburn; William C Reeves
Journal:  BMC Infect Dis       Date:  2003-06-19       Impact factor: 3.090

  3 in total

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